You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.
We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.
Your ideas influence the way we work, and your voice matters here.
As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.
Join us and build your future here.
What You'll Be Doing:
Create and format various basic to intermediate documents, utilizing internal processes and tools to perform the activities pertaining to electronic publishing and to meet required standards and technical requirements within specified timelines
Electronically publish components of Regulatory Agency submissions, including INDs and amendments, annual reports, safety reports, etc.
Work with relevant internal staff to ensure that source documents are received in a timely manner in order to support the generation of submissions
Perform the QC for all applications, amendments and supplements prior to submitting to Agency
Perform quality checks of others’ work
Participate in the implementation of new health agency guidelines and rules relevant to regulatory submissions
Participate in department projects that improve the department systems and processes
Assist in the review of Regulatory Operations work practices
Interact with clients, as needed
What We Are Searching For:
Bachelor’s degree, or international equivalent from an accredited institution, in Science/Technology, or an equivalent combination of education and experience
2-4 years of Regulatory Operations experience within the pharmaceutical or biotech industry
Basic to Intermediate experience using Microsoft Office and Adobe Professional
Ability to appropriately handle confidential and highly sensitive material
Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The annualized base pay for this role is between $60,000 - $100,000 USD. The actual salary will be influenced based on a variety of factors such as qualifications, skills, competencies, and proficiency for the role. We also offer comprehensive benefits packages, which may include health insurance, life insurance, retirement plan, paid time off, and an Employee Assistance Program.
Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status